Summary:

Job Responsibilities: 

1)  Works under limited supervision. Supervisor available to handle most unusual situations and review progress of work

2)  Conducts study tasks which are moderately complex to complex in accordance with established protocols or guidelines. Follows established guidelines in the review and collection of clinical data. May conduct screening of patients for inclusion in study based on predetermined criteria.

3)  Assists with/conducts informed consent process with PI/Sub-I available for questions. Assists with/conducts patient education regarding protocol and requirements. Assists with/conducts protocol evaluation and implementation planning.

4)  Develops, prepares, submits and maintains regulatory documents. Creates and maintains study and patient files in a highly accurate and organized manner. May develop study specific source and site...